meddevicedb.com FDA Device Reference

GRAHAM-FIELD ULTRASOUND LOTION

K944596 Class II Traditional
Decision Date
1995-06-07
Sponsor / Applicant
Chester Labs, Inc.

Technical Specification

510(k) Submission ID K944596
Product Code IMI
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5300
Decision Date 1995-06-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

GRAHAM-FIELD ULTRASOUND LOTION received FDA 510(k) clearance under submission number K944596, sponsored by Chester Labs, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Physical Medicine review panel. The statutory decision date of record is 1995-06-07.

Classification & Regulation

This clearance is catalogued under FDA product code IMI and 21 CFR 890.5300, within the Physical Medicine review panel as a Class II device.